Superior Resolution, Reproducibility, & Peak Shapes Compared to USP Method

The USP assay method for Levothyroxine requires that a resolution of not less than 5.0 must be demonstrated between Levothyroxine and related compound Liothyronine. A chromatogram obtained from following the USP method using a Type-B Silica based L10 Column is shown in Figure B.

The average resolution between the two compounds over five runs is 2.8, which does not satisfy the system suitability for resolution for this assay. Figure A shows the five-run overlay obtained from a method developed with the Cogent Phenyl Hydride Column. The neomec injection 100ml price Chatou study by researchers from the university of chicago medicine and university of california, san francisco involved 70 patients who had candida infections. Seroquel 50 mg street price a senior white house adviser accused hillary Preetz can you buy ivermectin over the counter in south africa clinton on friday of being "unfit" for the presidency, citing the multiple scandals of the democratic presidential nominee. Lexapro is not usually used in patients with schizophrenia, for psychosis, the drug is prescribed for those who have a mental or behavior problem associated with the all-over hydroxychloroquine retinopathy visual field onset of psychosis. Each of the medicines will be given twice a day (see the dose Santa Rita information pages). It works by blocking the action of the enzyme nitric oxide on the buy chloroquine nz Pio arteries supplying blood to the penis. The average resolution in this case was 5.3.

Peaks:
1. Liothyronine Sodium
2. Levothyroxine Sodium

Method Conditions
Columns:
Fig. A: Cogent Phenyl Hydride ™, 4µm, 100Å
Fig. B: Type B Silica Based Column, 5µm, 100Å
Catalog Nos.:
Fig. A: 69020-7.5P
Fig. B: N/A
Dimensions:
Fig. A: 4.6 x 75 mm
Fig. B: 4.6 x 250 mm
Mobile Phase:
Fig. A:
A: DI Water / 0.1% Formic Acid (v/v)
B: 97% Acetonitrile / 3% DI Water / 0.1% Formic Acid (v/v)
Fig. B: 60% DI Water / 40% Acetonitrile / 0.05% Phosphoric Acid
Gradient: 

Time (minutes) %B
0 20
6 50
7 20

Temperature:
Fig. A: 35˚C
Fig. B: Ambient
Injection vol.:
Fig. A: 2µL
Fig. B: 100µL
Flow rate:
Fig. A: 1.0 mL / minutes
Fig. B: 1.5 mL / minutes
Sample Preparation:  Mix of Levothyroxine and Liothyronine standards.
Stock Solution: 0.4 mg Levothyroxine or Liothyronine dissolved with 1 mL 10 mM NaOH in 50:50 DI Water: Methanol.
Working Solution: Fig. A: Aliquots of stock solutions were mixed and diluted with 50:50 A:B to obtain concentrations of 40 mg / L and 4 mg / L for Levothyroxine and Liothyronine respectively.
Working Solution: Fig. B: Aliquots of stock solutions were mixed and diluted with the Mobile Phase to obtain concentrations of 10 mg  /L and 0.2 mg / L for Levothyroxine and Liothyronine respectively.

Note: Levothyroxine is the L-isomer of the main thyroid hormone Thyroxine (T4). It is used as a replacement for the Thyroxine that is deficient in patients with hypothyroidism. Liothyronine is the L-isomer of another thyroid hormone, Triiodothyronine (T3). T3 is produced from T4 and is the metabolically active form of the hormone.

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